中国医药生物技术
中國醫藥生物技術
중국의약생물기술
CHINESE MEDICINAL BIOTECHNOLOGY
2015年
1期
11-17
,共7页
张浩%张彩霞%喻冬柯%邵荣光%何红伟
張浩%張綵霞%喻鼕柯%邵榮光%何紅偉
장호%장채하%유동가%소영광%하홍위
细胞系,肿瘤%细胞迁移抑制%基因表达谱%MAP激酶信号系统%G3BP
細胞繫,腫瘤%細胞遷移抑製%基因錶達譜%MAP激酶信號繫統%G3BP
세포계,종류%세포천이억제%기인표체보%MAP격매신호계통%G3BP
Cell line,tumor%Cell migration inhibition%Gene expression profiling%MAP kinase signaling system%G3BP
目的:探讨利用 siRNA和靶向 G3BP的多肽药物下调 G3BP后对多种肿瘤细胞迁移能力的影响。方法采用人纤维肉瘤 HT1080细胞、乳腺癌 MCF-7细胞以及人非小细胞肺癌 H1299细胞,应用 siRNA特异性干扰 G3BP后,通过划痕实验观察其对肿瘤细胞迁移能力的影响;用多肽药物 GAP161作用于肿瘤细胞后,利用划痕实验以及 Transwell迁移实验观察其对肿瘤细胞迁移能力的影响;在 MCF-7细胞中高表达 G3BP1,在 MDA-MB-231细胞中用 siRNA下调 G3BP1后,采用人全基因芯片分析 G3BP1高表达和低表达后的基因表达谱,并进行信号通路分析。结果 siRNA特异性下敲 G3BP1和 G3BP2后,HT1080、MCF-7和 H1299细胞的迁移能力显著降低。利用靶向 G3BP的特异性多肽药物 GAP161作用于多种肿瘤细胞后,肿瘤细胞的迁移能力显著下调。全基因组芯片分析表明:多个基因同时在 G3BP1高表达和低表达组中发生变化,该变化与细胞迁移相关的细胞黏附、整合素、MAPK 等信号通路有关。结论 G3BP下调后能够显著降低肿瘤细胞的迁移能力。靶向 G3BP的多肽药物具有显著抑制肿瘤细胞迁移的作用。下调或者高表达 G3BP后可通过下调或者上调多种与细胞黏附、整合素、MAPK 等信号通路相关基因发挥作用。
目的:探討利用 siRNA和靶嚮 G3BP的多肽藥物下調 G3BP後對多種腫瘤細胞遷移能力的影響。方法採用人纖維肉瘤 HT1080細胞、乳腺癌 MCF-7細胞以及人非小細胞肺癌 H1299細胞,應用 siRNA特異性榦擾 G3BP後,通過劃痕實驗觀察其對腫瘤細胞遷移能力的影響;用多肽藥物 GAP161作用于腫瘤細胞後,利用劃痕實驗以及 Transwell遷移實驗觀察其對腫瘤細胞遷移能力的影響;在 MCF-7細胞中高錶達 G3BP1,在 MDA-MB-231細胞中用 siRNA下調 G3BP1後,採用人全基因芯片分析 G3BP1高錶達和低錶達後的基因錶達譜,併進行信號通路分析。結果 siRNA特異性下敲 G3BP1和 G3BP2後,HT1080、MCF-7和 H1299細胞的遷移能力顯著降低。利用靶嚮 G3BP的特異性多肽藥物 GAP161作用于多種腫瘤細胞後,腫瘤細胞的遷移能力顯著下調。全基因組芯片分析錶明:多箇基因同時在 G3BP1高錶達和低錶達組中髮生變化,該變化與細胞遷移相關的細胞黏附、整閤素、MAPK 等信號通路有關。結論 G3BP下調後能夠顯著降低腫瘤細胞的遷移能力。靶嚮 G3BP的多肽藥物具有顯著抑製腫瘤細胞遷移的作用。下調或者高錶達 G3BP後可通過下調或者上調多種與細胞黏附、整閤素、MAPK 等信號通路相關基因髮揮作用。
목적:탐토이용 siRNA화파향 G3BP적다태약물하조 G3BP후대다충종류세포천이능력적영향。방법채용인섬유육류 HT1080세포、유선암 MCF-7세포이급인비소세포폐암 H1299세포,응용 siRNA특이성간우 G3BP후,통과화흔실험관찰기대종류세포천이능력적영향;용다태약물 GAP161작용우종류세포후,이용화흔실험이급 Transwell천이실험관찰기대종류세포천이능력적영향;재 MCF-7세포중고표체 G3BP1,재 MDA-MB-231세포중용 siRNA하조 G3BP1후,채용인전기인심편분석 G3BP1고표체화저표체후적기인표체보,병진행신호통로분석。결과 siRNA특이성하고 G3BP1화 G3BP2후,HT1080、MCF-7화 H1299세포적천이능력현저강저。이용파향 G3BP적특이성다태약물 GAP161작용우다충종류세포후,종류세포적천이능력현저하조。전기인조심편분석표명:다개기인동시재 G3BP1고표체화저표체조중발생변화,해변화여세포천이상관적세포점부、정합소、MAPK 등신호통로유관。결론 G3BP하조후능구현저강저종류세포적천이능력。파향 G3BP적다태약물구유현저억제종류세포천이적작용。하조혹자고표체 G3BP후가통과하조혹자상조다충여세포점부、정합소、MAPK 등신호통로상관기인발휘작용。
Objective To investigate the effect of G3BP down-regulation by siRNA or G3BP-targeted peptide GAP161 on tumor cell migration. Methods Effect of G3BP knockdown on tumor cell migration was examined by wound healing assay in HT1080, MCF-7 and H1299 cells. Effect of GAP161 on the migration of tumor cells was measured by wound healing assay and Transwell assay. Human whole genome oligonucleotide microarray was used to analyze the gene expression profiles in MCF-7 cells with G3BP1 over-expression and MDA-MB-231 cells with G3BP1 knockdown. Pathway analysis was then performed according to the microarray data. Results Down-regulation of G3BP1 and G3BP2 by specific siRNAs significantly inhibited cell migration in HT1080, MCF-7 and H1299 cells. GAP161 also significantly reduced the tumor cell migration ability. Whole genome microarray analysis showed that over-expression of G3BP1 and knockdown G3BP1 in MCF-7 and MDA-MB-231 cells, respectively, affected cell adhesion, integrin and MAPK signaling pathways in an opposite manner. Conclusion Knockdown of G3BP by siRNA significantly inhibited tumor cell migration. G3BP-targeted peptide G3BP1 markedly reduced the cell migration abilities. Over expression of G3BP1 could up-regulate genes expression associated with cell adhesion, integrin and MAPK signaling pathways, while down-regulation of G3BP1 exerts opposite effects.